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Endocrine
Endocrine
Endocrine
[Addison’s Disease]
Adrenal Glands
The three (3) classes of steroid hormones produced by the adrenal cortex are all
synthesized from cholesterol. These could be easily
remembered by representing the 3 functions of the
hormones of the adrenal cortex by the letter “S”, as salt,
sugar, and sex.
Because cortisol is so vital to health, the amount of cortisol produced by the adrenals is
precisely balanced. Like many other hormones, cortisol is regulated by the brain's hypothalamus
and the pituitary gland. First, the hypothalamus sends "releasing hormones" to the pituitary
gland. The pituitary responds by secreting other hormones that regulate growth, thyroid and
adrenal function, and sex hormones such as estrogen and testosterone. One of the pituitary's
main functions is to secrete ACTH (adrenocorticotropin), a hormone that stimulates the adrenal
glands. When the adrenals receive the pituitary's signal in the form of ACTH, they respond by
producing cortisol. Completing the cycle, cortisol then signals the pituitary to lower secretion of
ACTH.
DESCRIPTION
The disease is named for its discoverer, Dr. Thomas Addison, a British surgeon who described
adrenal insufficiency in 1849, though endocrine functions had yet to be explained.
It is a condition where the adrenal cortex (the outer layer of the adrenal gland that
produces mineralocorticoids, glucocorticoids, and androgens) is progressively
destroyed, resulting in decreased secretions of the hormones.
Other names
Adrenal Insufficiency
Adrenocortical Hypofunction
Hypocortisolism
Primary Adrenocortical Insufficiency
Chronic Adrenal Insufficiency
Chronic Primary Adrenal Insufficiency
Clinical Manifestations
The onset of Addison's disease is usually insidious. The client experiences mild fatigue,
languor, irritability, weight loss, nausea/vomiting, and postural hypotension weeks or months
before diagnosis of the disease. As the disorder progresses, manifestations intensify. The
development of clinical manifestations of adrenocortical insufficiency requires the loss of over
90% of both adrenal cortices.
Promotes appetite
Causes release of Inadequate release of epinephrine produces hypoglycemia
epinephrine from and hypotension
adrenal medulla
Assists in adaptation to Lowers resistance to stress and produces a “hyperresponse “
stress by increased to stressors: hypoglycemia, hypotension, hyperthermia
gluconeogenesis
releasing an anti
inflammatory response;
augmenting release of
catecholamines to
increase BP
ACTH regulates melanocyte Stimulates an increase MSH: increases skin and mucous
stimulating hormone membrane pigmentation, especially fingers, toes and sun
exposed body parts (skin appears bronzed)
Androgens Female oligomenorrhea or amenorrhea, decrease in body hair
Male No manifestations in males because testes produce adequate
quantities of sex hormones
In some cases, Addison's symptoms may present rapidly. This "acute adrenal failure" is
known as an Addisonian crisis (an exaggerated state of adrenal cortical insufficiency). An illness
or accident can aggravate the adrenal problems causing the Addisonian crisis, although the
most common cause is abrupt discontinuation of corticosteroid therapy without tapering the
dose. It may be provoked by physical stress, such as an injury, infection or illness.
An addisonian crisis is a life-threatening situation that results in low blood pressure, low
blood levels of sugar and high blood levels of potassium. This situation requires immediate
medical care and can be fatal if not treated quickly.
Types/Kinds/Variants
Epidemiology
Etiology
Pathophysiology
Adrenocortical Insufficiency
Signs& Symptoms